602-64-2,MFCD00019146
Catalog No.:AA003NTZ

602-64-2 | ANTHRACENE BROWN

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
99%
1 week  
$701.00   $491.00
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  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003NTZ
Chemical Name:
ANTHRACENE BROWN
CAS Number:
602-64-2
Molecular Formula:
C14H8O5
Molecular Weight:
256.2103
MDL Number:
MFCD00019146
SMILES:
O=C1c2ccccc2C(=O)c2c1c(O)c(c(c2)O)O
NSC Number:
31754
Properties
Properties
 
Form:
Solid  
MP:
>280°C (dec.)  
Storage:
2-8℃;Keep in dry area;  

Computed Properties
 
Complexity:
407  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.4  

Literature

Title: Tautomerism in 11-hydroxyaklavinone: a DFT study.

Journal: TheScientificWorldJournal 20120101

Title: Paramagnetic effects on the NMR spectra of 'diamagnetic' ruthenium(bis-phosphine)(bis-semiquinone) complexes.

Journal: Inorganic chemistry 20090615

Title: Chemical constituents isolated from Polygala japonica leaves and their inhibitory effect on nitric oxide production in vitro.

Journal: Journal of enzyme inhibition and medicinal chemistry 20090201

Title: Safety evaluation of topical applications of ethanol on the skin and inside the oral cavity.

Journal: Journal of occupational medicine and toxicology (London, England) 20080101

Title: Anthraquinones from Hedyotis capitellata.

Journal: Phytochemistry 20050501

Title: Synthesis and activity of substituted anthraquinones against a human filarial parasite, Brugia malayi.

Journal: Journal of medicinal chemistry 20050421

Title: Linkage and redox isomerism in ruthenium complexes of catecholate, semi-quinone, and o-acylphenolate ligands derived from tri- and tetrahydroxy-9,10-anthracenediones.

Journal: Inorganic chemistry 20010813

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SDS
Tags:602-64-2 Molecular Formula|602-64-2 MDL|602-64-2 SMILES|602-64-2 ANTHRACENE BROWN
Catalog No.: AA003NTZ
602-64-2,MFCD00019146
602-64-2 | ANTHRACENE BROWN
Pack Size: 100mg
Purity: 99%
1 week
$701.00 $491.00
Quantity
- +
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Technical Information
Catalog Number: AA003NTZ
Chemical Name: ANTHRACENE BROWN
CAS Number: 602-64-2
Molecular Formula: C14H8O5
Molecular Weight: 256.2103
MDL Number: MFCD00019146
SMILES: O=C1c2ccccc2C(=O)c2c1c(O)c(c(c2)O)O
NSC Number: 31754
Properties
Form: Solid  
MP: >280°C (dec.)  
Storage: 2-8℃;Keep in dry area;  
Complexity: 407  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 19  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.4  
Literature fold

Title: Tautomerism in 11-hydroxyaklavinone: a DFT study.

Journal: TheScientificWorldJournal20120101

Title: Paramagnetic effects on the NMR spectra of 'diamagnetic' ruthenium(bis-phosphine)(bis-semiquinone) complexes.

Journal: Inorganic chemistry20090615

Title: Chemical constituents isolated from Polygala japonica leaves and their inhibitory effect on nitric oxide production in vitro.

Journal: Journal of enzyme inhibition and medicinal chemistry20090201

Title: Safety evaluation of topical applications of ethanol on the skin and inside the oral cavity.

Journal: Journal of occupational medicine and toxicology (London, England)20080101

Title: Anthraquinones from Hedyotis capitellata.

Journal: Phytochemistry20050501

Title: Synthesis and activity of substituted anthraquinones against a human filarial parasite, Brugia malayi.

Journal: Journal of medicinal chemistry20050421

Title: Linkage and redox isomerism in ruthenium complexes of catecholate, semi-quinone, and o-acylphenolate ligands derived from tri- and tetrahydroxy-9,10-anthracenediones.

Journal: Inorganic chemistry20010813

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